Evidence map›Paper›PMID 28851744›Full record

ArticleGenetics2017

Identification of

Lauren J Donoghue, Alessandra Livraghi-Butrico, Kathryn M McFadden, Joseph M Thomas, Gang Chen, Barbara R Grubb, Wanda K O'Neal, Richard C Boucher, Samir N P Kelada

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. BPIFB1 loss alters airway mucus properties and diminishes mucociliary clearance.American journal of physiology. Lung cellular and molecular physiology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Intense light-elicited alveolar type 2-specific circadian PER2 protects from bacterial lung injury via BPIFB1.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  9. Article
  10. Article
  11. Baseline and innate immune response characterization of a Zfp30 knockout mouse strain.Mammalian genome : official journal of the International Mammalian Genome Society · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Host genetics in malaria: lessons from mouse studies.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Review
  20. Airway Mucus and Asthma: The Role of MUC5AC and MUC5B.Journal of clinical medicine · 2017
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Lauren J DonoghueDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599.
Alessandra Livraghi-ButricoMarsico Lung Institute, University of North Carolina, Chapel Hill, North Carolina 27599.
Kathryn M McFaddenDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599.
Joseph M ThomasDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599.
Gang ChenMarsico Lung Institute, University of North Carolina, Chapel Hill, North Carolina 27599.
Barbara R GrubbMarsico Lung Institute, University of North Carolina, Chapel Hill, North Carolina 27599.
Wanda K O'NealMarsico Lung Institute, University of North Carolina, Chapel Hill, North Carolina 27599.
Richard C BoucherMarsico Lung Institute, University of North Carolina, Chapel Hill, North Carolina 27599.
Samir N P KeladaDepartment of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599 samir_kelada@med.unc.edu.ORCID 0000-0003-2676-9232
University of North Carolina at Chapel Hill · USLung Institute · US

Funding

UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Stephanie Engel · 2001 to 2026
$36.3M
High-throughput targeted mutagenesis of mouse stem cell linesU01HG004080 · NHGRI · CHILDREN'S HOSPITAL & RES CTR AT OAKLAND · PI DE JONG, PIETER J. · 2006 to 2010
$28.1M
Vector CoreP30DK065988 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Martina Gentzsch · 2004 to 2026
$26.5M
The Biophysics of Mucus Hydration and Adhesion/CohesionP01HL108808 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BOUCHER, RICHARD CHARLES, PEDEN, DAVID B. · 2012 to 2021
$23.9M
Purinergic Control of CFTR-ENaC Interactions in Alveolar EpitheliaP01HL110873 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BOUCHER, RICHARD CHARLES · 2012 to 2016
$10.7M
Modeling heterogeneity for safe cancer prevention and detectionU01CA105417 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI THREADGILL, DAVID W. · 2004 to 2013
$6.7M
NRSA IN GENETICST32GM007092 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SEKELSKY, JEFF J. · 1985 to 2019
$5.9M
Systems Genetics Resource ConsortiumU01CA134240 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI THREADGILL, DAVID W. · 2007 to 2011
$5.4M
Synthesis of Effective and Safe Mucolytics for Pulmonary DiseaseUH3HL123645 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BOUCHER, RICHARD CHARLES · 2016 to 2018
$4.6M
Synthesis of Effective and Safe Mucolytics for Pulmonary DiseaseUH2HL123645 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BOUCHER, RICHARD CHARLES · 2014 to 2015
$2.9M
UNC Predoc Training Progr in Bioinformatics/Comp BiologyT32GM067553 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ELSTON, TIMOTHY C · 2005 to 2019
$2.5M
Gene-environment interactions in asthma in mice and humansZIAHG200361 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI COLLINS, FRANCIS S. · 2009 to 2012
$2.3M
Intramural NIH HHS ZIA HG200361NCI NIH HHS U01 CA105417NCI NIH HHS U01 CA134240NHGRI NIH HHS U01 HG004080NHLBI NIH HHS K23 HL089708NHLBI NIH HHS P01 HL108808NHLBI NIH HHS P01 HL110873NHLBI NIH HHS P50 HL107168NHLBI NIH HHS R01 HL116228NHLBI NIH HHS R01 HL122711NHLBI NIH HHS UH2 HL123645NHLBI NIH HHS UH3 HL123645NIDDK NIH HHS P30 DK065988NIEHS NIH HHS P30 ES010126NIEHS NIH HHS R01 ES024965NIGMS NIH HHS T32 GM007092NIGMS NIH HHS T32 GM067553
6 · The paper itself

Abstract

Mucus hyper-secretion is a hallmark feature of asthma and other muco-obstructive airway diseases. The mucin proteins MUC5AC and MUC5B are the major glycoprotein components of mucus and have critical roles in airway defense. Despite the biomedical importance of these two proteins, the loci that regulate them in the context of natural genetic variation have not been studied. To identify genes that underlie variation in airway mucin levels, we performed genetic analyses in founder strains and incipient lines of the Collaborative Cross (CC) in a house dust mite mouse model of asthma. CC founder strains exhibited significant differences in MUC5AC and MUC5B, providing evidence of heritability. Analysis of gene and protein expression of

Indexed as

Quantitative Trait LociAnimalsCarrier ProteinsCell LineFemaleMaleMiceMice, Inbred C57BLMucin 5ACMucin-5BRespiratory MucosaBPIFB1 protein, mouseCarrier ProteinsMuc5ac protein, mouseMuc5b protein, mouseMucin 5ACMucin-5BasthmaMUC5ACMUC5Bmucinsmucusquantitative trait locus (QTL)

Identifiers

PMID28851744
PMCPMC5629340
OpenAlexW2752107564

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.